ISO/TC 212

Reģistrācijas numurs (WIID)Projekta Nr.NosaukumsStatuss
79379ISO 16256:2021Clinical laboratory testing and in vitro diagnostic test systems — Broth micro-dilution reference method for testing the in vitro activity of antimicrobial agents against yeast fungi involved in infectious diseasesStandarts spēkā
51984ISO 19001:2013In vitro diagnostic medical devices — Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biologyStandarts spēkā
69802ISO 20166-2:2018Analyses de diagnostic moléculaire in vitro — Spécifications relatives aux processus préanalytiques pour les tissus fixés au formol et inclus en paraffine (FFPE) — Partie 2: Protéines extraitesStandarts spēkā
42022ISO 15194:2009In vitro diagnostic medical devices — Measurement of quantities in samples of biological origin — Requirements for certified reference materials and the content of supporting documentationStandarts spēkā
77070ISO/TS 23824:2024Medical laboratories — Guidance on application of ISO 15189 in anatomic pathologyStandarts spēkā
72191ISO 15190:2020Laboratoires de biologie médicale — Exigences pour la sécuritéStandarts spēkā
67217ISO 20186-1:2019Analyses de diagnostic moléculaire in vitro — Spécifications relatives aux processus préanalytiques pour le sang total veineux — Partie 1: ARN cellulaire extraitStandarts spēkā
85349ISO 18704:2026Molecular in vitro diagnostic examinations — Requirements and recommendations for pre-examination processes for urine and other body fluids — Isolated cell-free DNAStandarts spēkā
81506ISO 5649:2024Laboratoires médicaux — Concepts et spécifications relatifs à la conception, au développement, à la mise en œuvre et à l’utilisation des tests développés en laboratoireStandarts spēkā
87680ISO/TS 22583:2024Requirements and recommendations for supervisors and operators of point-of-care testing (POCT) equipmentStandarts spēkā
Attēlo no 111. līdz 120. no pavisam 146 ieraksta(-iem).